LaO_x(OH)_y supported platinum catalysts for CO oxidation:Deactivation by formation of lanthanum carbonate |
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Authors: | Luozhen Jiang Junxiang Chen Rui Si |
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Affiliation: | 1. Shanghai Institute of Applied Physics, Chinese Academy of Sciences, Shanghai 201204, China;2. Shanghai Synchrotron Radiation Facility, Zhangjiang Laboratory, Shanghai 201204, China;3. Division of China, TILON Group Technology Limited, Shanghai 200090, China;4. University of Chinese Academy of Sciences, Beijing 100049, China |
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Abstract: | ![]() Platinum catalyst for CO oxidation has been studied for decades,due to its high activity and good stability.In this work,we prepared three different lantha num oxide or hydroxide supports(LaO_x(OH)_y),and deposited platinum(Pt) with 0.5 at% via an impregnation approach to synthesize Pt/LaO_x(OH)_y catalysts.However,we find that these catalysts perform a poor stability for the CO oxidation reaction.The fresh and used samples were comprehensively characterized by multiple techniques including power X-ray diffraction(XRD),X-ray absorption fine structure(XAFS),transmission electron microscopy(TEM),temperature-programmed reduction by carbon monoxide(CO-TPR) and thermogravimetric analysis(TGA),to demonstrate that the oxidized platinum atoms or clusters,without any component of Pt-Pt metallic bond,are highly dispersed on the surface of LaO_x(OH)_y.Furthermore,the as-formed lanthanum carbonate(La_2 O_2 CO_3) during the exposure to ambient circumstances or in the reaction atmosphere of CO+O_2,severely impair the reactivity of Pt/LaO_x(OH)_y.On the basis of the obtained experimental results,we have drawn a conclusion that the oxidized PtO_x atoms or Pt_xO_y clusters are the active species for CO oxidation,while the formation of lanthanum carbonate is the origin of deactivation on reactivity. |
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Keywords: | Platinum catalyst Lanthanum oxide Lanthanum hydroxide CO oxidation Structure–activity relationship Rare earths |
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